Evidence map›Paper›PMID 40624141›Full record

ArticleScientific reports2025

Structure-based design of an antibacterial peptide from the Myotoxin II sequence, evaluating its effectiveness against Gram-negative bacteria and its safety.

Tatiana Huertas, Diana Millán, Angela V Fonseca-Benítez, James Guevara-Pulido

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Brief history of ophidiology and ophidism in Colombia.Transactions of the Royal Society of Tropical Medicine and Hygiene · 2026
    Review
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Tatiana HuertasQuímica Farmacéutica, INQA, Universidad El Bosque, Bogotá, Colombia.
Diana MillánFacultad de Medicina, GIBAT, Universidad El Bosque, Bogotá, Colombia.
Angela V Fonseca-BenítezQuímica Farmacéutica, INQA, Universidad El Bosque, Bogotá, Colombia.
James Guevara-PulidoQuímica Farmacéutica, INQA, Universidad El Bosque, Bogotá, Colombia. joguevara@unbosque.edu.co.ORCID http://orcid.org/0000-0001-9134-3719

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial resistance poses a significant public health challenge, particularly for pathogens prioritized by the World Health Organization, such as carbapenem-resistant Escherichia coli. There has been growing interest in exploring animal toxins as potential alternatives to antibiotics. This study centers on the rational design of an antibiotic peptide based on the sequence 115-129 from Myotoxin II, sourced from the venom of the snake Bothrops asper. We modified the original sequence 20 times using molecular docking and found that peptide sequence 20 (KHWYKHYRH) exhibited the highest affinity energy of - 7.6 kcal/mol for lipopolysaccharide (LPS). The in vitro potency was assessed against E. coli, with an IC

Indexed as

Anti-Bacterial AgentsGram-Negative BacteriaPeptidesAmino Acid SequenceAnimalsBothropsDrug DesignEscherichia coliHemolysisHumansKlebsiella pneumoniaeMicrobial Sensitivity TestsMolecular Docking SimulationAnti-Bacterial AgentsPeptidesE. coliGram-negative bacteriaLipopolysaccharideMolecular dockingMyotoxin II

Identifiers

PMID40624141
PMCPMC12234863

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.